Molecules 2007, 12(7), 1420-1429; doi:10.3390/12071420
Article

An Efficient and Rapid Synthetic Route to Biologically Interesting Pyranochalcone Natural Products

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Received: 29 June 2007; in revised form: 10 July 2007 / Accepted: 10 July 2007 / Published: 12 July 2007
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: An efficient and concise total synthesis of naturally occurring pyranochalcones was achieved from readily available 2,4-dihydroxyacetophenone and 2,4-dihydroxy-6- methoxyacetophenone. The key steps in the synthetic strategy were ethylenediamine diacetate-catalyzed benzopyran formation and aldol reactions.
Keywords: Ethylenediamine diacetate;Pyranyl ring formation;Pyranochalcone natural products;Aldol reaction
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MDPI and ACS Style

Lee, Y.R.; Wang, X.; Xia, L. An Efficient and Rapid Synthetic Route to Biologically Interesting Pyranochalcone Natural Products. Molecules 2007, 12, 1420-1429.

AMA Style

Lee YR, Wang X, Xia L. An Efficient and Rapid Synthetic Route to Biologically Interesting Pyranochalcone Natural Products. Molecules. 2007; 12(7):1420-1429.

Chicago/Turabian Style

Lee, Yong R.; Wang, Xue; Xia, Likai. 2007. "An Efficient and Rapid Synthetic Route to Biologically Interesting Pyranochalcone Natural Products." Molecules 12, no. 7: 1420-1429.

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